Ex vivo expansion of hematopoietic cells from umbilical cord blood for clinical transplantation

被引:39
作者
Conrad, PD [1 ]
Emerson, SG
机构
[1] Childrens Hosp Philadelphia, Dept Pediat, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Div Hematol, Philadelphia, PA 19104 USA
[3] Childrens Hosp Philadelphia, Div Oncol, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[5] Univ Penn, Div Hematol Oncol, Philadelphia, PA 19104 USA
关键词
stem cell transplantation; neutropenia; thrombocytopenia;
D O I
10.1002/jlb.64.2.147
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stem cell transplantation (SCT) has achieved significant therapeutic success over the last 10 years, providing a viable treatment option for many previously incurable diseases. However, several inherent limitations of the procedure have restricted its widespread use. These include: lack of sufficient donors for all recipients, a period of bone marrow (BM) aplasia leading to severe, prolonged neutropenia and thrombocytopenia, and the potential for tumor contamination in autologous SCT. Umbilical cord blood (UCB) provides a unique, and potentially more successful, approach to alleviating these limitations. Ex vivo manipulation of hematopoietic stem (HSCs) and progenitor cells (HPCs) derived from UCB using a Liquid culture system has revealed that the primitive HSCs from UCB are not identical to their BM counterparts. In fact, these cells may derive from a more primitive stem cell compartment. Ultimately; successful engraftment of UCB HSCs manipulated in an ex vivo environment may lead to a larger number of these life-saving procedures being performed and the full potential of SCT realized.
引用
收藏
页码:147 / 155
页数:9
相关论文
共 67 条
[1]   CD34-positive cells isolated from cryopreserved peripheral-blood progenitor cells can be expanded ex vivo and used for transplantation with little or no toxicity [J].
Alcorn, MJ ;
Holyoake, TL ;
Richmond, L ;
Pearson, C ;
Farrell, E ;
Kyle, B ;
Dunlop, DJ ;
Fitzsimons, E ;
Steward, WP ;
Pragnell, IB ;
Franklin, IM .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (06) :1839-1847
[2]   CELLULAR INTERRELATIONSHIPS DURING INVITRO GRANULOPOIESIS [J].
ALLEN, TD ;
DEXTER, TM .
DIFFERENTIATION, 1976, 6 (03) :191-194
[3]  
BARNETT MJ, 1994, BLOOD, V84, P724
[4]   Quantitative analysis reveals expansion of human hematopoietic repopulating cells after short-term ex vivo culture [J].
Bhatia, M ;
Bonnet, D ;
Kapp, U ;
Wang, JCY ;
Murdoch, B ;
Dick, JE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (04) :619-624
[5]   Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice [J].
Bhatia, M ;
Wang, JCY ;
Kapp, U ;
Bonnet, D ;
Dick, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5320-5325
[6]  
BRUGGER W, 1993, BLOOD, V81, P2579
[7]   RETRACTED: RECONSTITUTION OF HEMATOPOIESIS AFTER HIGH-DOSE CHEMOTHERAPY BY AUTOLOGOUS PROGENITOR CELLS GENERATED EX-VIVO (RETRACTED ARTICLE. SEE VOL 345, PG 64, 2001) [J].
BRUGGER, W ;
HEIMFELD, S ;
BERENSON, RJ ;
MERTELSANN, R ;
KANZ, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (05) :283-287
[8]   QUANTITATIVE MEASUREMENTS OF OXYGEN TENSION IN NORMAL TISSUES AND IN THE TUMOURS OF PATIENTS BEFORE AND AFTER RADIOTHERAPY [J].
CATER, DB ;
SILVER, IA .
ACTA RADIOLOGICA, 1960, 53 (03) :233-256
[9]  
COULOMBEL L, 1983, BLOOD, V62, P291
[10]   FLT3 ligand preserves the ability of human CD34(+) progenitors to sustain long-term hematopoiesis in immune-deficient mice after ex vivo retroviral-mediated transduction [J].
Dao, MA ;
Hannum, CH ;
Kohn, DB ;
Nolta, JA .
BLOOD, 1997, 89 (02) :446-456